APA (7th ed.) Citation

T, H., C, S., E, S., JG, B., J, C., C, F., . . . L, T. (2024). De novo variants in ATXN7L3 lead to developmental delay, hypotonia and distinctive facial features. Brain : a journal of neurology, 147(8), 2732. https://doi.org/10.1093/brain/awae160

Chicago Style (17th ed.) Citation

T, Harel, et al. "De Novo Variants in ATXN7L3 Lead to Developmental Delay, Hypotonia and Distinctive Facial Features." Brain : A Journal of Neurology 147, no. 8 (2024): 2732. https://doi.org/10.1093/brain/awae160.

MLA (9th ed.) Citation

T, Harel, et al. "De Novo Variants in ATXN7L3 Lead to Developmental Delay, Hypotonia and Distinctive Facial Features." Brain : A Journal of Neurology, vol. 147, no. 8, 2024, p. 2732, https://doi.org/10.1093/brain/awae160.